PD0325901 (PD325901)

产品编号: DC1056 Featured
PD0325901 (PD325901)
结构式
391210-10-9
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中国地区超过5000个高品质化合物库存
应用领域
PD0325901是选择性,可渗透细胞的 MEK 抑制剂, IC50为0.33 nM。
Cas No.: 391210-10-9
名称: (R)-N-(2,3-dihydroxypropoxy)-3,4-difluoro-2-(2-fluoro-4-iodophenylamino)benzamide
别名: PD-0325901 , PD-325901
SMILES: C1=CC(=C(C=C1I)F)NC2=C(C=CC(=C2F)F)C(=O)NOC[C@@H](CO)O
分子式: C16H14F3In2O4
分子量: 482.19
纯度:
保存条件: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description:
In Vivo:
In Vitro:
References: PD-0325901, a MEK inhibitor, is an orally bioavailable, synthetic organic molecule targeting mitogen-activated protein kinase kinase (MAPK/ERK kinase or MEK) with potential antineoplastic activity. MEK inhibitor PD325901, a derivative of MEK inhibitor CI-1040, selectively binds to and inhibits MEK, which may result in the inhibition of the phosphorylation and activation of MAPK/ERK and the inhibition of tumor cell proliferation. The dual specific threonine/tyrosine kinase MEK is a key component of the RAS/RAF/MEK/ERK signaling pathway that is frequently activated in human tumors. Check For active clinical trials or closed clinical trials using this agent. (NCI Thesaurus). For the detailed information about the solubility of PD0325901 (PD325901) in water, the solubility of PD0325901 (PD325901) in DMSO, the solubility of PD0325901 (PD325901) in PBS buffer, the animal experiment(test) of PD0325901 (PD325901),the in vivo,in vitro and clinical trial test of PD0325901 (PD325901),the cell experiment(test) of PD0325901 (PD325901),the IC50, EC50 and Affinity of PD0325901 (PD325901), please contact DC Chemicals.
Kinase Assay:
Cell Assay:
Animal Administration:
References:
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
产品编号 产品名称 应用领域
DC1056 PD0325901 (PD325901) PD0325901是选择性,可渗透细胞的 MEK 抑制剂, IC50为0.33 nM。